Colon Cancer: Gene >> HPRT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298556 |
| Start |
134475189:134475189(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs387906725
|
| CDS Mutation |
c.143G>A |
| AA Mutation |
p.Arg48His(p.R48H) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298556 |
| Start |
134498658:134498658(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.583T>A |
| AA Mutation |
p.Tyr195Asn(p.Y195N) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
Rectum Cancer: Gene >> HPRT1
| Mutation ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000298556 |
| Start |
134493586:134493586(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs137852484
|
| CDS Mutation |
c.481G>T |
| AA Mutation |
p.Ala161Ser(p.A161S) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| Mutation ID |
2 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000298556 |
| Start |
134493585:134493585(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
rs148780933
|
| CDS Mutation |
c.480C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |
|